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Terminated

Weck Electrosurgical Coagulation Suction Tube (with stylet), REF 809600, Cannula 6'' 11 French, Rx Only, Sterile, Weck A Teleflex Company, Manufactured for: Weck Closure Systems, 2917 Weck Drive, Research Triangle park, NC 27709, USA.

FDA Recall Z-0418-05 · Posted 2005-01-25

Recalling FirmWeck
Recall StatusTerminated
Product CodeGDO
Date Initiated2003-05-21
Date Terminated2005-01-31
Product Quantity667 units

Reason for Recall

Some stylets were not bent sufficiently during the packaging process to preclude them from sliding back into the cannula during shipment.

Firm Action

Consignees were notified by letter sent via Federal Express on/about 05/21/2003.

Root Cause

Other

Distribution Pattern

Nationwide

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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